ERMIS Vagotomy Set - Indonesia BPOM Medical Device Registration
ERMIS Vagotomy Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10804220009. The device is manufactured by ERMIS MEDTECH GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DYRSA INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ERMIS MEDTECH GMBHCountry of Origin
Germany
Authorized Representative
PT. DYRSA INTERNATIONALAR Address
JL. SUKARAJA II NO. 277A RT.01 RW. 06 SUKARAJA CICENDO, BANDUNG
Registration Date
Feb 16, 2022
Expiry Date
Sep 01, 2026
Product Type
Gastroenterology-Surgical Urology Equipment
Manual gastroenterology-urology surgical instrument and accessories.
Non Electromedic Non Sterile
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